Organic electroluminescent device

ABSTRACT

A high-efficiency, high-durability organic electroluminescent device, particularly a phosphorescent organic electroluminescent device is provided by using an organic compound of excellent characteristics that exhibits excellent hole-injecting/transporting performance and has high triplet exciton confining capability with an electron blocking ability, and that has high stability in the thin-film state and high luminous efficiency. 
     The organic electroluminescent device includes a pair of electrodes, and a plurality of organic layers sandwiched between the pair of electrodes and including a light emitting layer and an electron blocking layer, wherein a compound of the following general formula (1) having a carbazole ring structure is used as a constituent material of the electron blocking layer and the light emitting layer.

TECHNICAL FIELD

The present invention relates to organic electroluminescent devices(hereinafter, simply referred to as “organic EL devices”), preferredself light-emitting devices for various display devices. Specifically,the invention relates to organic EL devices that use compounds having acarbazole ring structure.

BACKGROUND ART

The organic EL device is a self-emitting device, and has been activelystudied for their brighter, superior viewability and ability to displayclearer images compared with the liquid crystal device.

In 1987, C. W. Tang et al. at Eastman Kodak developed a laminatedstructure device using materials assigned with different roles,realizing practical applications of an organic EL device with organicmaterials. These researchers laminated tris(8-hydroxyquinoline)aluminum(an electron-transporting phosphor; hereinafter, simply Alq₃), and ahole-transporting aromatic amine compound, and injected the both chargesinto the phosphor layer to cause emission in order to obtain a highluminance of 1,000 cd/m² or more at a voltage of 10 V or less (see, forexample, Patent Documents 1 and 2).

To date, various improvements have been made for practical applicationsof the organic EL device. In order to realize high efficiency anddurability, various roles are further subdivided to provide anelectroluminescent device that includes an anode, a hole injectionlayer, a hole transport layer, a light emitting layer, an electrontransport layer, an electron injection layer, and a cathode successivelyformed on a substrate (see, for example, Non-Patent Document 1).

Further, there have been attempts to use triplet excitons for furtherimprovements of luminous efficiency, and use of phosphorescent materialshave been investigated (see, for example, Non-Patent Document 2).

The light emitting layer can also be fabricated by doping acharge-transporting compound, generally called a host material, with aphosphor or a phosphorescent material. As described in the foregoinglecture preprints, selection of organic materials in an organic ELdevice greatly influences various device characteristics, includingefficiency and durability.

In an organic EL device, the charges injected from the both electrodesrecombine at the light emitting layer to cause emission. The probabilityof hole-electron recombination can be improved by improving the holeinjectability and the electron blocking performance of blocking theinjected electrons from the cathode, and high luminous efficiency can beobtained by confining the excitons generated in the light emittinglayer. The role of the hole transport material is therefore important,and there is a need for a hole transport material that has high holeinjectability, high hole mobility, high electron blocking performance,and high durability to electrons.

The aromatic amine derivatives described in Patent Documents 1 and 2 areknown examples of the hole transport materials used for the organic ELdevice. These compounds include a compound known to have an excellenthole mobility of 10⁻³ cm²/Vs or higher. However, the compound isinsufficient in terms of electron blocking performance, and some of theelectrons pass through the light emitting layer. Accordingly,improvements in luminous efficiency cannot be expected.

Arylamine compounds of the following formulae having a substitutedcarbazole structure (for example, Compounds A, B, and C) are proposed asimprovements over the foregoing compounds (see, for example, PatentDocuments 3 to 5).

In an attempt to improve the device luminous efficiency, there have beendeveloped devices that use phosphorescent materials to generatephosphorescence, specifically that make use of the emission from thetriplet excitation state. According to the excitation state theory,phosphorescent materials are expected to greatly increase luminousefficiency about four times as much as that of the conventionalfluorescence.

In 1999, M. A. Baldo et al. at Princeton University realized 8% luminousefficiency with a phosphorescent device using an iridium complex, agreat improvement over the conventional external quantum efficiency. Thephosphorescent device has been actively developed ever since.

Improving the luminous efficiency of the phosphorescent device requiresuse of materials of high excitation triplet energy level (hereinafter,simply “T₁”) for the host material. However, there is a report that useof materials with high T₁ is also necessary for the hole transportmaterial to confine the triplet excitons (see, for example, Non-PatentDocument 3). Further, the green phosphorescent materialtris(phenylpyridyl)iridium (hereinafter, simply “Ir(ppy)₃”) representedby the following formula has a T₁ of 2.42 eV.

Because N,N′-diphenyl-N,N′-di(α-naphthyl)benzidine (hereinafter, simply“α-NPD”) has a T₁ of 2.29 eV, sufficient confinement of the tripletexcitons cannot be expected with α-NPD. Higher luminous efficiency isthus obtained using 1,1-bis[4-(di-4-tolylamino)phenyl]cyclohexane(hereinafter, simply “TAPC”) of the following formula having a higher T₁value of 2.9 eV (see, for example, Non-Patent Document 4).

However, the TAPC has low hole mobility, and its ionization potential(work function) 5.8 eV is not appropriate for a hole transport material.

The ionization potential (work function) of Compound A is 5.5 eV, a moreappropriate value compared to the ionization potential of the TAPC. Itis expected that this, combined with the high T₁ of 2.9 eV, wouldprovide sufficient confinement of the triplet excitons. However, becausethe compound has low hole mobility, the product device has high drivingvoltage, and the luminous efficiency cannot be said as sufficient (see,for example, Non-Patent Document 5). Accordingly, there is a need formaterials having a high T₁ value and high hole mobility that can be usednot only as a hole injection layer or a hole transport layer butpreferably as an electron blocking layer, in order to obtain aphosphorescent device having improved luminous efficiency.

CITATION LIST Patent Documents

-   Patent Document 1: JP-A-8-048656-   Patent Document 2: Japanese Patent Number 3194657-   Patent Document 3: JP-A-8-003547-   Patent Document 4: JP-A-2006-151979-   Patent Document 5: WO2008/62636-   Patent Document 6: JP-A-2007-022986

Non-Patent Documents

-   Non-Patent Document 1: The Japan Society of Applied Physics, 9th    lecture preprints, pp. 55 to 61 (2001)-   Non-Patent Document 2: The Japan Society of Applied Physics, 9th    lecture preprints, pp. 23 to 31 (2001)-   Non-Patent Document 3: J. Appl. Phys., 12, 95, 7798 (2004)-   Non-Patent Document 4: Organic EL Display, 89 (2004), Tokitoh,    Adachi, Murata, Ohmsha-   Non-Patent Document 5: Appl. Phys. Lett., 93, 063306 (2008)-   Non-Patent Document 6: Helvetica Chimica Acta., vol. 89, 1123 (2006)-   Non-Patent Document 7: J. Org. Chem., 60, 7508 (1995)-   Non-Patent Document 8: Synth. Commun., 11, 513 (1981)-   Non-Patent Document 9: Jikken Kagaku Kouza 7, 4th ed., pp. 384-398    (1992), The Chemical Society of Japan, Maruzen-   Non-Patent Document 10: Organic EL Symposium, the 1st Regular    presentation Preprints, 19 (2005)-   Non-Patent Document 11: Appl. Phys. Lett., 93, 133312 (2008)

SUMMARY OF THE INVENTION Problems that the Invention is to Solve

It is an object of the present invention to provide a high-efficient,high-durable organic EL device, particularly a phosphorescent organic ELdevice, using an organic compound of excellent characteristics thatexhibits excellent hole-injecting/transporting performance and has hightriplet exciton confining capability with an electron blocking ability,and that has high stability in the thin-film state and high luminousefficiency.

Some of the physical properties of the organic compound used for theorganic EL device of the present invention include (1) good holeinjection characteristics, (2) high hole mobility, (3) high T₁ value,(4) excellent electron blocking ability, (5) stability in the thin-filmstate, and (6) excellent heat resistance. Some of the physicalproperties of the organic EL device to be provided by the presentinvention include (1) high luminous efficiency and high powerefficiency, (2) low turn on voltage, and (3) low actual driving voltage.

Means for Solving the Problems

In order to achieve the foregoing objects, the present inventors focusedon the high T₁ value, the excellent electron blocking performance andexcellent hole transporting ability, and the excellent heat resistanceand excellent thin film stability of a carbazole ring structure, andproduced various test organic EL devices by designing, selecting, andchemically synthesizing compounds linked to a carbazole ring structure.The present invention was completed after thorough evaluations of thedevice characteristics.

Specifically, the present invention provides the following organic ELdevices.

1) An organic EL device that includes a pair of electrodes, and aplurality of organic layers sandwiched between the pair of electrodesand including a light emitting layer and an electron blocking layer,wherein a compound of the following general formula (1) having acarbazole ring structure is used as a constituent material of theelectron blocking layer.

In the formula, R1, R2, R3, R4, R5, and R6 may be the same or different,and represent a fluorine atom, a chlorine atom, cyano, trifluoromethyl,nitro, linear or branched alkyl of 1 to 6 carbon atoms, cycloalkyl of 5to 10 carbon atoms, linear or branched alkyloxy of 1 to 6 carbon atoms,cycloalkyloxy of 5 to 10 carbon atoms, a substituted or unsubstitutedaromatic hydrocarbon group, a substituted or unsubstituted aromaticheterocyclic group, a substituted or unsubstituted condensed polycyclicaromatic group, or substituted or unsubstituted aryloxy. r1, r4, and r5represent 0 or an integer of 1 to 4. r2, r3, and r6 represent 0 or aninteger of 1 to 3. n represents 0 or an integer of 1. Ar1, Ar2, and Ar3may be the same or different, and represent a substituted orunsubstituted aromatic hydrocarbon group, a substituted or unsubstitutedaromatic heterocyclic group, or a substituted or unsubstituted condensedpolycyclic aromatic group.

2) An organic EL device of 1), wherein Ar2 in the general formula (1) isa monovalent group of the following general formula (2) or (3).

In the formula, R7 and R8 may be the same or different, and represent afluorine atom, a chlorine atom, cyano, trifluoromethyl, nitro, linear orbranched alkyloxy of 1 to 6 carbon atoms, cycloalkyloxy of 5 to 10carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group,a substituted or unsubstituted aromatic heterocyclic group, asubstituted or unsubstituted condensed polycyclic aromatic group, orsubstituted or unsubstituted aryloxy. r7 represents 0 or an integer of 1to 4, and r8 represents 0 or an integer of 1 to 3. B represents adivalent group of a substituted or unsubstituted aromatic hydrocarbon, adivalent group of a substituted or unsubstituted aromatic heterocyclicring, or a divalent group of a substituted or unsubstituted condensedpolycyclic aromatic. Ar4 represents a substituted or unsubstitutedaromatic hydrocarbon group, a substituted or unsubstituted aromaticheterocyclic group, or a substituted or unsubstituted condensedpolycyclic aromatic group.

In the formula, R9 and R10 may be the same or different, and represent afluorine atom, a chlorine atom, cyano, trifluoromethyl, nitro, linear orbranched alkyl of 1 to 6 carbon atoms, cycloalkyl of 5 to 10 carbonatoms, linear or branched alkyloxy of 1 to 6 carbon atoms, cycloalkyloxyof 5 to 10 carbon atoms, a substituted or unsubstituted aromatichydrocarbon group, a substituted or unsubstituted aromatic heterocyclicgroup, a substituted or unsubstituted condensed polycyclic aromaticgroup, or substituted or unsubstituted aryloxy. r9 and r10 represent 0or an integer of 1 to 3. C represents a divalent group of a substitutedor unsubstituted aromatic hydrocarbon, a divalent group of a substitutedor unsubstituted aromatic heterocyclic ring, or a divalent group of asubstituted or unsubstituted condensed polycyclic aromatic. Ar5represents a substituted or unsubstituted aromatic hydrocarbon group, asubstituted or unsubstituted aromatic heterocyclic group, or asubstituted or unsubstituted condensed polycyclic aromatic group. W, X,Y, and Z represent a carbon atom or a nitrogen atom, where only one ofW, X, Y, and Z is a nitrogen atom, and, in this case, the nitrogen atomdoes not have the substituent R9.

3) An organic EL device of 1) or 2), wherein the light emitting layercontains a phosphorescent light-emitting material.

4) An organic EL device that includes a pair of electrodes, and aplurality of organic layers sandwiched between the pair of electrodesand including a phosphorescent light-emitting material-containing lightemitting layer and an electron blocking layer, wherein the compound ofthe general formula (1) having a carbazole ring structure is used as aconstituent material of the light emitting layer.

5) An organic EL device of 3) or (4), wherein the phosphorescentlight-emitting material is a metal complex that contains iridium orplatinum.

Specific examples of the “linear or branched alkyl of 1 to 6 carbonatoms” or the “cycloalkyl of 5 to 10 carbon atoms” represented by R1 toR10 in general formulae (1) to (3) include methyl, ethyl, n-propyl,isopropyl, n-butyl, isobutyl, tert-butyl, n-pentyl, isopentyl,neopentyl, n-hexyl, cyclopentyl, cyclohexyl, 1-adamantyl, and2-adamantyl.

Specific examples of the “linear or branched alkyloxy of 1 to 6 carbonatoms” or the “cycloalkyloxy of 5 to 10 carbon atoms” represented by R1to R10 in general formulae (1) to (3) include methyloxy, ethyloxy,n-propyloxy, isopropyloxy, n-butyloxy, tert-butyloxy, n-pentyloxy,n-hexyloxy, cyclopentyloxy, cyclohexyloxy, cycloheptyloxy,cyclooctyloxy, 1-adamantyloxy, and 2-adamantyloxy.

Specific examples of the “aromatic hydrocarbon group”, the “aromaticheterocyclic group”, or the “condensed polycyclic aromatic group” in the“substituted or unsubstituted aromatic hydrocarbon group”, the“substituted or unsubstituted aromatic heterocyclic group”, or the“substituted or unsubstituted condensed polycyclic aromatic group”represented by R1 to R10 or Ar1 to Ar5 in general formulae (1) to (3)include phenyl, biphenylyl, terphenylyl, naphthyl, anthryl, phenanthryl,fluorenyl, indenyl, pyrenyl, acenaphthenyl, fluoranthenyl,triphenylenyl, pyridyl, furanyl, pyranyl, thienyl, quinolyl,isoquinolyl, benzofuranyl, benzothienyl, indolyl, carbazolyl,benzooxazolyl, benzothiazolyl, quinoxalyl, benzoimidazolyl, pyrazolyl,dibenzofuranyl, dibenzothienyl, and carbolinyl, of which phenyl,biphenylyl, terphenylyl, fluorenyl, carbazolyl, and carbolinyl arepreferable. Preferably, the “condensed polycyclic aromatic” has 20 orless carbon atoms, because T₁ becomes smaller as the number of carbonatoms in the “condensed polycyclic aromatic” increases.

Specific examples of the “substituent” in the “substituted aromatichydrocarbon group”, the “substituted aromatic heterocyclic group”, orthe “substituted condensed polycyclic aromatic group” represented by R1to R10 or Ar1 to Ar5 in general formulae (1) to (3) include a fluorineatom, a chlorine atom, cyano, trifluoromethyl, nitro, linear or branchedalkyl of 1 to 6 carbon atoms, cycloalkyl of 5 to 10 carbon atoms, linearor branched alkenyl of 2 to 6 carbon atoms, linear or branched alkyloxyof 1 to 6 carbon atoms, cycloalkyloxy of 5 to 10 carbon atoms, phenyl,naphthyl, anthryl, styryl, phenoxy, tolyloxy, benzyloxy, andphenethyloxy. These substituents may be further substituted.

Specific examples of the “aryloxy” in the “substituted or unsubstitutedaryloxy” represented by R1 to R10 or Ar1 to Ar5 in general formulae (1)to (3) include phenoxy, biphenylyloxy, terphenylyloxy, naphthyloxy,anthryloxy, phenanthryloxy, fluorenyloxy, indenyloxy, and pyrenyloxy.

Specific examples of the “substituent” in the “substituted aryloxy”represented by R1 to R10 or Ar1 to Ar5 in general formulae (1) to (3)include a fluorine atom, a chlorine atom, cyano, trifluoromethyl, nitro,linear or branched alkyl of 1 to 6 carbon atoms, cycloalkyl of 5 to 10carbon atoms, linear or branched alkyloxy of 1 to 6 carbon atoms,cycloalkyloxy of 5 to 10 carbon atoms, phenyl, naphthyl, anthryl,styryl, phenoxy, tolyloxy, benzyloxy, and phenethyloxy. Thesesubstituents may be further substituted.

Specific examples of the “divalent group of an aromatic hydrocarbon”,the “divalent group of an aromatic heterocyclic ring”, or the “divalentgroup of a condensed polycyclic aromatic” in the “divalent group of asubstituted or unsubstituted aromatic hydrocarbon”, the “divalent groupof a substituted or unsubstituted aromatic heterocyclic ring”, or the“divalent group of a substituted or unsubstituted condensed polycyclicaromatic” represented by B or C in general formulae (2) to (3) includephenylene, biphenylene, terphenylene, tetrakisphenylene, naphthylene,anthrylene, phenanthrylene, fluorenylene, phenanthrolylene, indenylene,pyrenylene, acenaphthenylene, fluoranthenylene, triphenylenylene,pyridinylene, pyrimidinylene, quinolylene, isoquinolylene, indolylene,carbazolylene, quinoxalylene, benzoimidazolylene, pyrazolylene,naphthyridinylene, phenanthrolinylene, acridinylene, thienylene,benzothienylene, and dibenzothienylene.

Specific examples of the “substituent” in the “divalent group of asubstituted aromatic hydrocarbon”, the “divalent group of a substitutedaromatic heterocyclic ring”, or the “divalent group of a substitutedcondensed polycyclic aromatic” represented by B or C in general formulae(2) to (3) include a fluorine atom, a chlorine atom, cyano,trifluoromethyl, nitro, linear or branched alkyl of 1 to 6 carbon atoms,cycloalkyl of 5 to 10 carbon atoms, linear or branched alkenyl of 2 to 6carbon atoms, linear or branched alkyloxy of 1 to 6 carbon atoms,cycloalkyloxy of 5 to 10 carbon atoms, phenyl, naphthyl, anthryl,styryl, phenoxy, tolyloxy, benzyloxy, and phenethyloxy. Thesesubstituents may be further substituted.

Among the compounds of the general formula (1) having a carbazole ringstructure, the compounds of the following general formula (1′) having acarbazole ring structure with n=0, and the compounds of the followinggeneral formula (1″) having a carbazole ring structure with n=1 arepreferably used for an organic EL device.

In the formula, R1, R2, R3, R4, R7, and R8 may be the same or different,and represent a fluorine atom, a chlorine atom, cyano, trifluoromethyl,nitro, linear or branched alkyl of 1 to 6 carbon atoms, cycloalkyl of 5to 10 carbon atoms, linear or branched alkyloxy of 1 to 6 carbon atoms,cycloalkyloxy of 5 to 10 carbon atoms, a substituted or unsubstitutedaromatic hydrocarbon group, a substituted or unsubstituted aromaticheterocyclic group, a substituted or unsubstituted condensed polycyclicaromatic group, or substituted or unsubstituted aryloxy. r1, r4, and r7represent 0 or an integer of 1 to 4. r2, r3, and r8 represent 0 or aninteger of 1 to 3. B represents a divalent group of a substituted orunsubstituted aromatic hydrocarbon, a divalent group of a substituted orunsubstituted aromatic heterocyclic ring, or a divalent group of asubstituted or unsubstituted condensed polycyclic aromatic. Ar3 and Ar4may be the same or different, and represent a substituted orunsubstituted aromatic hydrocarbon group, a substituted or unsubstitutedaromatic heterocyclic group, or a substituted or unsubstituted condensedpolycyclic aromatic group.

In the formula, R1, R2, R3, R4, R5, and R6 may be the same or different,and represent a fluorine atom, a chlorine atom, cyano, trifluoromethyl,nitro, linear or branched alkyl of 1 to 6 carbon atoms, cycloalkyl of 5to 10 carbon atoms, linear or branched alkyloxy of 1 to 6 carbon atoms,cycloalkyloxy of 5 to 10 carbon atoms, a substituted or unsubstitutedaromatic hydrocarbon group, a substituted or unsubstituted aromaticheterocyclic group, a substituted or unsubstituted condensed polycyclicaromatic group, or substituted or unsubstituted aryloxy. r4 and r5represent 0 or an integer of 1 to 4. r1, r2, r3, and r6 represent 0 oran integer of 1 to 3. Ar1, Ar2, and Ar3 may be the same or different,and represent a substituted or unsubstituted aromatic hydrocarbon group,a substituted or unsubstituted aromatic heterocyclic group, or asubstituted or unsubstituted condensed polycyclic aromatic group.

The compounds of general formula (1) having a carbazole ring structureused for the organic EL device of the present invention are highlycapable of confining triplet excitons, and have superior electronblocking ability and heat resistance, and a stable thin-film state.

The compounds of general formula (1) having a carbazole ring structureused for the organic EL device of the present invention also may be usedas a constituent material of the hole injection layer and/or holetransport layer of the organic EL device, particularly a phosphorescentorganic EL device. With the compounds having high hole injectability,high mobility, high T₁ value, and high electron stability, the tripletexcitons generated in the light emitting layer containing thephosphorescent light-emitting material can be confined, and theprobability of hole-electron recombination can be improved. Thisimproves the luminous efficiency, and lowers driving voltage and thusimproves the durability of the organic EL device.

The compounds of general formula (1) having a carbazole ring structureused for the organic EL device of the present invention also may be usedas a constituent material of the electron blocking layer of the organicEL device, particularly a phosphorescent organic EL device. With thematerial having high triplet exciton confining capability and excellenthole transportability with high stability in the thin-film state, thedriving voltage lowers and the current resistance improves whilemaintaining high luminous efficiency. As a result, the maximum emissionluminance of the organic EL device improves.

The compounds of general formula (1) having a carbazole ring structureused for the organic EL device of the present invention also may be usedas a constituent material of the light emitting layer of the organic ELdevice, particularly a phosphorescent organic EL device. The compoundshave excellent hole transportability and a wide band gap, and can thusbe used as the host material of the light emitting layer in order toform the light emitting layer by carrying a phosphorescent materialcalled a dopant. In this way, an organic EL device can be realized thathas a low driving voltage and improved luminous efficiency.

The organic EL device of the present invention uses the compound havinga carbazole ring structure, wherein the compound has high hole mobilityand excellent triplet exciton confining capability while having a stablethin-film state. In this way, high efficiency and high durability arerealized.

Advantage of the Invention

The compound having a carbazole ring structure used for the organic ELdevice of the present invention is useful as a constituent material ofthe electron blocking layer or light emitting layer of the organic ELdevice, particularly a phosphorescent organic EL device. The compoundhas excellent triplet exciton confining capability, and excels in heatresistance while having a stable thin-film state. The organic EL deviceof the present invention has high luminous efficiency and high powerefficiency, and can thus lower the actual driving voltage of the device.Further, the turn on voltage can be lowered to improve durability.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a 1H-NMR chart of the compound of Example 1 of the presentinvention (Compound 4).

FIG. 2 is a 1H-NMR chart of the compound of Example 2 of the presentinvention (Compound 25).

FIG. 3 is a diagram representing the configuration of the organic ELdevices of Examples 6 and 7.

FIG. 4 is a diagram representing the configuration of the organic ELdevices of Comparative Examples 1 and 2.

MODE FOR CARRYING OUT THE INVENTION

The compounds having a carbazole ring structure used in the presentinvention may be synthesized by using known methods (see, for example,Patent Document 3), or by using, for example, the following method.First, a monobromocarbazole such as 3-bromo-9-arylcarbazole, or adibromocarbazole such as 3,6-dibromo-9-arylcarbazole is synthesized bythe bromination of a carbazole substituted with an aryl group at thecorresponding ninth position, using, for example, N-bromosuccinimide(see, for example, Non-Patent Document 6). The boronic acid or boratesynthesized by the reaction of the resulting monobromocarbazole with acompound such as pinacolborane or bis(pinacolato)diboron (see, forexample, Non-Patent Document 7) can then be reacted withdibromocarbazole or monobromocarbazole in a cross-coupling reaction suchas Suzuki coupling (see, for example, Non-Patent Document 8) tosynthesize bis(N-aryl-9′H-carbazol-3′-yl)-9-aryl-9H-carbazole or(N-aryl-9′H-carbazol-3′-yl)-9H-carbazole. The(N-aryl-9′H-carbazol-3′-yl)-9-halogenoaryl-carbazole obtained by thecondensation reaction (such as Ullmann reaction) of the(N-aryl-9′H-carbazol-3′-yl)-9H-carbazole with various dihalogenoarylenescan be reacted with 3-boronic acid or borate of 9-arylcarbazole in across-coupling reaction such as Suzuki coupling (see, for example,Non-Patent Document 8) to synthesize a compound having a carbazole ringstructure.

The following presents specific examples of preferred compounds amongthe compounds of general formula (1) having a carbazole ring structure.The present invention, however, is not restricted to these compounds.

These compounds were purified by methods such as column chromatography,adsorption using, for example, a silica gel, activated carbon, oractivated clay, and recrystallization or crystallization using asolvent. The compounds were identified by NMR analysis. Glass transitionpoint (Tg) and work function were taken for the measurement of physicalproperties. Glass transition point (Tg) can be used as an index ofstability in the thin-film state, and the work function as an index ofhole transportability.

The glass transition point (Tg) was measured using a powder, using ahigh-sensitive differential scanning calorimeter DSC3100S produced byBruker AXS.

For the measurement of work function, a 100 nm-thick thin film wasfabricated on an ITO substrate, and an atmosphere photoelectronspectrometer AC-3 produced by Riken Keiki Co., Ltd. was used.

The T₁ values of these compounds can be calculated from the measuredphosphorescence spectrum. The phosphorescence spectrum can be measuredusing a commercially available spectrophotometer. Typically, thephosphorescence spectrum is measured by shining excitation light underlow temperature on the compound dissolved in a solvent (see, forexample, Non-Patent Document 9), or by shining excitation light underlow temperature on the compound formed into a thin film by being vapordeposited on a silicon substrate (see, for example, Patent Document 6).T₁ can be calculated by conversion into a light energy value accordingto the equation below from the wavelength of the first peak on theshorter wavelength side of the phosphorescence spectrum, or from thewavelength at the rise of the spectrum on the shorter wavelength side.T₁ is used as an index of triplet exciton confinement by thephosphorescent material.E(eV)=hc/λ  [Equation 1]

In the equation, E represents the light energy value, h the Planck'sconstant (6.63×10⁻³⁴ Js), c the speed of light (3.00×10⁸ m/s), and λ thewavelength (nm) at the rise of the phosphorescence spectrum on theshorter wavelength side. 1 eV=1.60×10⁻¹⁹ J.

The organic EL device of the present invention may have a structureincluding an anode, a hole injection layer, a hole transport layer, anelectron blocking layer, a light emitting layer, a hole blocking layer,an electron transport layer, and a cathode successively formed on asubstrate, optionally with an electron injection layer between theelectron transport layer and the cathode. Some of the organic layers inthis multilayer structure may be omitted.

Each of the light emitting layer, the hole transport layer, and theelectron transport layer may have a laminate structure of two or morelayers.

Electrode materials with a large work function, such as ITO and gold,are used as the anode of the organic EL device of the present invention.The hole injection layer of the organic EL device of the presentinvention may be made of a material, the examples of which includeporphyrin compounds as represented by copper phthalocyanine,starburst-type triphenylamine derivatives, various triphenylaminetetramers, accepting heterocyclic compounds such as hexacyanoazatriphenylene, and coating-type polymer materials, in addition to thecompounds of general formula (1) having a carbazole ring structure ofthe present invention. These materials may be formed into a thin film byusing a vapor deposition method, or other known methods such as spincoating and an inkjet method.

Examples of the material used for the hole transport layer of theorganic EL device of the present invention include benzidine derivatives(such as TPD, α-NPD, and N,N,N′,N′-tetrabiphenylylbenzidine), TAPC, andvarious triphenylamine trimers and tetramers, in addition to thecompounds of general formula (1) having a carbazole ring structure ofthe present invention. These may be individually deposited for filmforming, or may be used as a single layer deposited as a mixture withother materials, or as a laminate of individually deposited layers, alaminate of layers deposited as a mixture, or a laminate of layersdeposited by being mixed with an individually deposited layer. Examplesof the material used for the hole injection/transport layer includecoating-type polymer materials such as poly(3,4-ethylenedioxythiophene)(hereinafter, simply “PEDOT”)/poly(styrene sulfonate) (hereinafter,simply “PSS”). These materials may be formed into a thin-film by using avapor deposition method, or other known methods such as spin coating andan inkjet method.

Further, the hole injection layer or the hole transport layer may be oneobtained by the P-doping of material such as trisbromophenylaminehexachloroantimony in the material commonly used for these layers.Further, for example, polymer compounds having a TPD structure as a partof the compound structure also may be used.

Examples of the material used for the electron blocking layer of theorganic EL device of the present invention include compounds having anelectron blocking effect, including, for example, carbazole derivativessuch as 4,4′,4″-tri(N-carbazolyl)triphenylamine (hereinafter, simply“TCTA”), 9,9-bis[4-(carbazol-9-yl)phenyl]fluorene,1,3-bis(carbazol-9-yl)benzene (hereinafter, simply “mCP”), and2,2-bis(4-carbazol-9-ylphenyl)adamantane (hereinafter, simply “Ad-Cz”);and compounds having a triphenylsilyl group and a triarylaminestructure, as represented by9-[4-(carbazol-9-yl)phenyl]-9-[4-(triphenylsilyl)phenyl]-9H-fluorene, inaddition to the compounds of general formula (1) having a carbazole ringstructure of the present invention. These may be individually depositedfor film forming, or may be used as a single layer deposited as amixture with other materials, or as a laminate of individually depositedlayers, a laminate of layers deposited as a mixture, or a laminate oflayers deposited by being mixed with an individually deposited layer.These materials may be formed into a thin-film by using a vapordeposition method, or other known methods such as spin coating and aninkjet method.

Examples of the material used for the light emitting layer of theorganic EL device of the present invention include various metalcomplexes, anthracene derivatives, bis(styryl)benzene derivatives,pyrene derivatives, oxazole derivatives, and polyparaphenylene vinylenederivatives, in addition to quinolinol derivative metal complexes suchas Alq₃. Further, the light emitting layer may be configured from a hostmaterial and a dopant material. Examples of the host material includethiazole derivatives, benzimidazole derivatives, and polydialkylfluorene derivatives, in addition to the foregoing light-emittingmaterials, and the compounds of general formula (1) having a carbazolering structure of the present invention. Examples of the dopant materialinclude quinacridone, coumarin, rubrene, perylene, derivatives thereof,benzopyran derivatives, rhodamine derivatives, and aminostyrylderivatives. These may be individually deposited for film forming, ormay be used as a single layer deposited as a mixture with othermaterials, or as a laminate of individually deposited layers, a laminateof layers deposited as a mixture, or a laminate of layers deposited bybeing mixed with an individually deposited layer.

Further, the light-emitting material may be phosphorescentlight-emitting material. Phosphorescent materials as metal complexes ofmetals such as iridium and platinum may be used as the phosphorescentlight-emitting material. Examples of the phosphorescent materialsinclude green phosphorescent materials such as Ir(ppy)₃, bluephosphorescent materials such as FIrpic and FIr6, and red phosphorescentmaterials such as Btp₂Ir(acac). Here, the compounds of general formula(1) having a carbazole ring structure of the present invention may beused as the hole injecting and transporting host material, in additionto carbazole derivatives such as 4,4′-di (N-carbazolyl)biphenyl(hereinafter, simply “CBP”), TCTA, and mCP. Compounds such asp-bis(triphenylsilyl)benzene (hereinafter, simply “UGH2”), and2,2′,2″-(1,3,5-phenylene)-tris(1-phenyl-1H-benzimidazole) (hereinafter,simply “TPBI”) represented by the following formula may be used as theelectron transporting host material.

In order to avoid concentration quenching, the doping of the hostmaterial with the phosphorescent light-emitting material shouldpreferably be made by co-evaporation in a range of 1 to 30 weightpercent with respect to the whole light emitting layer.

A device including a light emitting layer fabricated with the compoundof general formula (1) having a carbazole ring structure used for theorganic EL device of the present invention may be produced as a laminatewith an adjacently laminated light emitting layer fabricated by using acompound of a different work function as the host material (see, forexample, Non-Patent Documents 10 and 11).

These materials may be formed into a thin-film by using a vapordeposition method, or other known methods such as spin coating and aninkjet method.

The hole blocking layer of the organic EL device of the presentinvention may be formed by using hole blocking compounds such as variousrare earth complexes, oxazole derivatives, triazole derivatives, andtriazine derivatives, in addition to the metal complexes ofphenanthroline derivatives such as bathocuproin (hereinafter, simply“BCP”), and the metal complexes of quinolinol derivatives such asaluminum(III) bis(2-methyl-8-quinolinate)-4-phenylphenolate(hereinafter, simply “BAlq”). These materials may also serve as thematerial of the electron transport layer. These may be individuallydeposited for film forming, or may be used as a single layer depositedas a mixture with other materials, or as a laminate of individuallydeposited layers, a laminate of layers deposited as a mixture, or alaminate of layers deposited by being mixed with an individuallydeposited layer. These materials may be formed into a thin-film by usinga vapor deposition method, or other known methods such as spin coatingand an inkjet method.

Examples of the material used for the electron transport layer of theorganic EL device of the present invention include various metalcomplexes, triazole derivatives, triazine derivatives, oxadiazolederivatives, thiadiazole derivatives, carbodiimide derivatives,quinoxaline derivatives, phenanthroline derivatives, and silolederivatives, in addition to quinolinol derivative metal complexes suchas Alq₃ and BAlq. These may be individually deposited for film forming,or may be used as a single layer deposited as a mixture with othermaterials, or as a laminate of individually deposited layers, a laminateof layers deposited as a mixture, or a laminate of layers deposited bybeing mixed with an individually deposited layer. These materials may beformed into a thin-film by using a vapor deposition method, or otherknown methods such as spin coating and an inkjet method.

Examples of the material used for the electron injection layer of theorganic EL device of the present invention include alkali metal salts(such as lithium fluoride, and cesium fluoride), alkaline earth metalsalts (such as magnesium fluoride), and metal oxides (such as aluminumoxide). However, the electron injection layer may be omitted uponpreferably selecting the electron transport layer and the cathode.

The electron injection layer or the electron transport layer may be oneobtained by the N-doping of metals such as cesium in the materialscommonly used for these layers.

The cathode of the organic EL device of the present invention may bemade of an electrode material having a low work function (such asaluminum), or an alloy of an electrode material having an even lowerwork function (such as a magnesium-silver alloy, a magnesium-indiumalloy, or an aluminum-magnesium alloy).

The thickness of each layer in the organic EL device of the presentinvention is not particularly limited, and is typically from 0.1 nm to 1μm, preferably 0.3 nm to 500 nm, because defects such as pinholes arelikely to occur when the layers are thin, and because applied voltagetends to increase with thick layers.

The following describes an embodiment of the present invention in moredetail based on Examples. The present invention, however, is notrestricted to the following Examples.

EXAMPLE 1 Synthesis of3,6-bis(9′-phenyl-9′H-carbazol-3-yl)-9-phenyl-9H-carbazole (Compound 4)

3,6-Dibromo-9-phenyl-9H-carbazole (1.6 g),9-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxabororan-2-yl)-9 H-carbazole(2.4 g), toluene (20 ml), ethanol (5 ml), and a 2 M potassium carbonateaqueous solution (6 ml) were added to a nitrogen-substituted reactionvessel, and aerated with nitrogen gas for 30 minutes under ultrasonicwaves. The mixture was heated after addingtetrakis(triphenylphosphine)palladium (0.23 g), and stirred at 74° C.for 4 hours. After adding toluene (80 ml), the mixture was heated, andfurther stirred at 70° C. for 1 hour. The mixture was then cooled to 40°C., and the insolubles were removed by filtration. The filtrate was thenconcentrated under reduced pressure to obtain a black crude product.Toluene (100 ml) was added to dissolve the crude product, and thesolution was subjected to adsorptive purification with a silica gel(28.9 g), and concentrated under reduced pressure to obtain a yellowishwhite powder. The yellowish white powder was repeatedly purified twiceby recrystallization using toluene/methanol to obtain a brownish whitepowder of 3,6-bis(9-phenyl-9′H-carbazol-3-yl)-9-phenyl-9H-carbazole(Compound 4; 1.76 g; yield 60.9%).

The structure of the resulting brownish white powder was identified byNMR. The 1H-NMR measurement result is presented in FIG. 1.

1H-NMR (CDCl₃) detected 35 hydrogen signals, as follows. δ(ppm)=8.56(2H), 8.49 (2H), 8.24-8.26 (2H), 7.79-7.81 (4H), 7.62-7.67 (12H),7.43-7.55 (11H), 7.30-7.33 (2H).

EXAMPLE 2 Synthesis of9′-phenyl-9-[4-(9-phenyl-9H-carbazol-3-yl)-phenyl]-9H,9′H-[3,3′]bicarbazolyl(Compound 25)

9-Phenyl-9H,9′H-[3,3′]bicarbazolyl (12.9 g), 4-bromo-iodobenzene (13.4g), a copper powder (0.64 g), potassium carbonate (8.34 g), sodiumbisulfite (0.49 g), and orthodichlorobenzene (50 ml) were added to anitrogen-substituted reaction vessel, heated, and stirred at 170° C. for19.5 hours. The mixture was cooled to 90° C., and dissolved after addingtoluene (200 ml). After removing the insolubles by filtration, thefiltrate was concentrated under reduced pressure, and crystallized frommethanol (50 ml) to obtain a white powder of9-(4-bromophenyl)-9′-phenyl-9H,9′H-[3,3′]bicarbazolyl (17.30 g; yield97%).

The resulting 9-(4-bromophenyl)-9′-phenyl-9H,9′H-[3,3′]bicarbazolyl(17.00 g),9-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxabororan-2-yl)-9H-carbazole(12.25 g), toluene (160 ml), ethanol (40 ml), and a 2 M potassiumcarbonate aqueous solution (23 ml) were added to a nitrogen-substitutedreaction vessel, and aerated with nitrogen gas for 30 minutes underultrasonic waves. After adding tetrakis(triphenylphosphine)palladium(1.74 g), the mixture was heated, and stirred at 72° C. for 12.5 hours.The mixture was allowed to cool to room temperature, and extraction wasperformed by adding toluene (100 ml) and water (150 ml) thereto. Theorganic layer was dried over magnesium sulfate, and concentrated underreduced pressure to obtain a black crude product. The crude product waspurified by column chromatography (carrier: silica gel; eluent:hexane/toluene) to obtain a pale yellowish white powder of9′-phenyl-9-[4-(9-phenyl-9H-carbazol-3-yl)-phenyl]-9H,9′H-[3,3′]bicarbazolyl(10.44 g; yield 48%).

The structure of the resulting pale yellowish white powder wasidentified by NMR. The 1H-NMR measurement result is presented in FIG. 2.

1H-NMR (THF-d₈) detected 35 hydrogen signals, as follows.δ(ppm)=7.25-7.31 (3H), 7.36-7.44 (5H), 7.48-7.53 (5H), 7.58 (1H),7.64-7.69 (8H), 7.73-7.76 (2H), 7.81-7.85 (3H), 8.04-8.08 (2H),8.26-8.30 (3H), 8.56-8.61 (3H).

EXAMPLE 3

The glass transition points of the compounds used in the presentinvention were determined using a high-sensitive differential scanningcalorimeter DSC 3100S produced by Bruker AXS.

Glass transition point Compound of Example 1 of the present invention142.5° C. Compound of Example 2 of the present invention 151.4° C.

The compounds used in the present invention have glass transition pointsof 100° C. or higher, demonstrating that the compounds used in thepresent invention have a stable thin-film state.

EXAMPLE 4

A 100 nm-thick vapor-deposited film was fabricated on an ITO substrateusing the compounds used in the present invention, and the work functionwas measured using an atmosphere photoelectron spectrometer (Model AC-3produced by Riken Keiki Co., Ltd.).

Work function Compound of Example 1 of the present invention 5.44 eVCompound of Example 2 of the present invention 5.49 eV

As the results show, the compounds used in the present invention havedesirable energy levels compared to the work function 5.4 eV of commonhole transport materials such as α-NPD and TPD, and thus possessdesirable hole transportability.

EXAMPLE 5

A 1.0×10⁻⁵ mol/L 2-methyltetrahydrofuran solution was prepared for thecompounds used in the present invention. The prepared solution wasplaced in a designated quartz tube, and aerated with pure nitrogen toremove the oxygen content. The tube was plugged with a septum rubber toprevent mixing with oxygen. After being cooled to 77 K, the solution wasirradiated with excitation light to measure the phosphorescencespectrum, using a spectrofluorometer FluoroMax-4 produced by Horiba Ltd.The wavelength of the first peak on the shorter wavelength side of thephosphorescence spectrum was taken, and the wavelength value wasconverted to light energy to calculate T₁.

T₁ Compound of Example 1 of the present invention 2.74 eV Compound ofExample 2 of the present invention 2.71 eV FIrpic 2.62 eV Ir(ppy)₃ 2.42eV CBP 2.56 eV α-NPD 2.29 eV

As can be seen, the compounds used in the present invention have higherT₁ values than commonly used blue phosphorescent material FIrpic, greenphosphorescent material Ir(ppy)₃, commonly used host material CBP, andcommonly used hole transport material α-NPD, and thus have sufficientcapability for the confinement of the triplet excitons excited in thelight emitting layer.

EXAMPLE 6

The organic EL device, as illustrated in FIG. 3, was fabricated from ahole transport layer 3, an electron blocking layer 4, a light emittinglayer 5, a hole blocking layer 6, an electron transport layer 7, anelectron injection layer 8, and a cathode (aluminum electrode) 9successively formed by vapor deposition on a glass substrate 1 that hadbeen provided beforehand with an ITO electrode as a transparent anode 2.

Specifically, the glass substrate 1 having ITO (thickness 150 nm) formedthereon was washed with an organic solvent, and subjected to an oxygenplasma treatment to wash the surface. The glass substrate with the ITOelectrode was then installed in a vacuum vapor deposition apparatus, andthe pressure was reduced to 0.001 Pa or less. This was followed byformation of the hole transport layer 3 by forming α-NPD over thetransparent anode 2 in a thickness of 40 nm. The electron blocking layer4 was then formed on the hole transport layer 3 by forming the compoundof Example 1 of the present invention (Compound 4) in a thickness of 10nm. Thereafter, the light emitting layer 5 was formed on the electronblocking layer 4 by forming TPBI and Ir(ppy)₃ in a thickness of 20 nmusing dual vapor deposition at a deposition rate ratio ofTPBI:Ir(ppy)₃=92:8. The hole blocking layer 6 was then formed on thelight emitting layer 5 by forming BCP in a thickness of 10 nm. Then, theelectron transport layer 7 was formed on the hole blocking layer 6 byforming Alq₃ in a thickness of 30 nm. The electron injection layer 8 wasthen formed on the electron transport layer 7 by forming lithiumfluoride in a thickness of 0.5 nm. Finally, the cathode 9 was formed byvapor depositing aluminum in a thickness of 150 nm. The characteristicsof the organic EL device thus fabricated were measured in an atmosphereat ordinary temperature. Table 1 summarizes the results of the emissioncharacteristics measurements performed by applying a DC voltage to theorganic EL device.

EXAMPLE 7

An organic EL device was fabricated under the same conditions used inExample 6, except that the compound 53 of the structural formula belowwas used as the material of the hole transport layer 3 of Example 6. Thecharacteristics of the organic EL device thus fabricated were measuredin an atmosphere at ordinary temperature. Table 1 summarizes the resultsof the emission characteristics measurements performed by applying a DCvoltage to the organic EL device.

COMPARATIVE EXAMPLE 1

For comparison, an organic EL device was fabricated under the sameconditions used in Example 6, except that the hole transport layer 3 wasformed in a thickness of 50 nm, and that the electron blocking layer 4was omitted. The characteristics of the organic EL device thusfabricated were measured in an atmosphere at ordinary temperature. Table1 summarizes the results of the emission characteristics measurementsperformed by applying a DC voltage to the organic EL device.

COMPARATIVE EXAMPLE 2

For comparison, an organic EL device was fabricated under the sameconditions used in Example 7, except that the hole transport layer 3 wasformed in a thickness of 50 nm, and that the electron blocking layer 4was omitted. The characteristics of the organic EL device thusfabricated were measured in an atmosphere at ordinary temperature. Table1 summarizes the results of the emission characteristics measurementsperformed by applying a DC voltage to the organic EL device.

TABLE 1 Hole transport layer Voltage Luminance Current efficiency Powerefficiency material/electron [V] [cd/m²] [cd/A] [lm/W] blocking layermaterial (@ 10 mA/cm²) (@ 10 mA/cm²) (@ 10 mA/cm²) (@ 10 mA/cm²) Example6 α-NPD/Compound 4 5.77 2604 26.07 14.21 Example 7 Compound 53/ 5.682943 29.48 16.30 Compound 4 Comparative α-NPD/None 6.54 1931 19.33 9.29Example 1 Comparative Compound 53/None 5.89 1896 18.98 10.23 Example 2

As can be seen in Table 1, the driving voltage upon passing a currentwith a current density of 10 mA/cm² was 5.77 V or 5.68 V for thecompound of Example 1 of the present invention (Compound 4) used as thematerial of the electron blocking layer, lower than 6.54 V or 5.89 V ofwhen α-NPD or compound 53 was used as the material of the hole transportlayer without using the compound of Example 1 of the present invention(Compound 4) as the material of the electron blocking layer. Further,the emission luminance, current efficiency, and power efficiency allgreatly improved in the devices in which the compound of Example 1 ofthe present invention (Compound 4) was used as the material of theelectron blocking layer.

The results of turn on voltage measurements using the foregoing organicEL devices are presented below.

Hole transport layer Turn on material/electron voltage Organic EL deviceblocking layer material [V] Example 6 α-NPD/Compound 4 2.8 Example 7Compound 53/Compound 4 2.8 Comparative Example 1 α-NPD/None 2.9Comparative Example 2 Compound 53/None 2.9

It can be seen that the turn on voltage was lower in Examples 6 and 7 inwhich the compound of Example 1 of the present invention (Compound 4)was used as the material of the electron blocking layer than inComparative Examples 1 and 2 in which the compound of Example 1 of thepresent invention (Compound 4) was not used as the material of theelectron blocking layer.

As these results demonstrate, the organic EL devices in which thecompound of general formula (1) having a carbazole ring structure usedin the present invention is used as the material of the electronblocking layer can have improved emission luminance, luminousefficiency, and power efficiency, and a lower actual driving voltage.

INDUSTRIAL APPLICABILITY

The organic EL device produced by using the compound of general formula(1) having a carbazole ring structure can have high emission luminance,high luminous efficiency, and high power efficiency, and can have a lowactual driving voltage to improve durability. There are potentialapplications for, for example, home electronic appliances andilluminations.

DESCRIPTION OF REFERENCE NUMERALS AND SIGNS

-   1 Glass substrate-   2 Transparent anode-   3 Hole transport layer-   4 Electron blocking layer-   5 Light emitting layer-   6 Hole blocking layer-   7 Electron transport layer-   8 Electron injection layer-   9 Cathode

The invention claimed is:
 1. An organic electroluminescent devicecomprising a pair of electrodes, and a plurality of organic layerssandwiched between the pair of electrodes and including a phosphorescentlight-emitting material-containing light emitting layer and an electronblocking layer, wherein a compound of the following general formula (1)having a carbazole ring structure is used as a constituent material ofthe electron blocking layer,

wherein R1, R2, R3, R4, R5, and R6 may be the same or different, andrepresent a fluorine atom, a chlorine atom, cyano, trifluoromethyl,nitro, linear or branched alkyl of 1 to 6 carbon atoms, cycloalkyl of 5to 10 carbon atoms, linear or branched alkyloxy of 1 to 6 carbon atoms,cycloalkyloxy of 5 to 10 carbon atoms, a substituted or unsubstitutedaromatic hydrocarbon group, a substituted or unsubstituted aromaticheterocyclic group, a substituted or unsubstituted condensed polycyclicaromatic group, or substituted or unsubstituted aryloxy, r1, r4, and r5represent 0 or an integer of 1 to 4, r2, r3, and r6 represent 0 or aninteger of 1 to 3, n represents 1, Ar1, Ar2, and Ar3 may be the same ordifferent, and represent a substituted or unsubstituted aromatichydrocarbon group, a substituted or unsubstituted aromatic heterocyclicgroup, or a substituted or unsubstituted condensed polycyclic aromaticgroup, and wherein, when Ar1 is a substituted aromatic hydrocarbongroup, the substituent is a fluorine atom, a chlorine atom, cyano,trifluoromethyl, nitro, cycloalkyl of 5 to 10 carbon atoms, linear orbranched alkenyl of 2 to 6 carbon atoms, linear or branched alkyloxy of1 to 6 carbon atoms, cycloalkyloxy of 5 to 10 carbon atoms, phenyl,naphthyl, anthryl, styryl, phenoxy, tolyloxy, benzyloxy, orphenethyloxy, each of which may be further substituted.
 2. The organicelectroluminescent device of claim 1 in which the compound having acarbazole ring structure is used as a constituent material of theelectron blocking layer, wherein Ar2 in the general formula (1) is amonovalent group represented by the following general formula (2) or(3),

wherein R7 and R8 may be the same or different, and represent a fluorineatom, a chlorine atom, cyano, trifluoromethyl, nitro, linear or branchedalkyl of 1 to 6 carbon atoms, cycloalkyl of 5 to 10 carbon atoms, linearor branched alkyloxy of 1 to 6 carbon atoms, cycloalkyloxy of 5 to 10carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group,a substituted or unsubstituted aromatic heterocyclic group, asubstituted or unsubstituted condensed polycyclic aromatic group, orsubstituted or unsubstituted aryloxy, r7 represents 0 or an integer of 1to 4, r8 represents 0 or an integer of 1 to 3, B represents a divalentgroup of a substituted or unsubstituted aromatic hydrocarbon, a divalentgroup of a substituted or unsubstituted aromatic heterocyclic ring, or adivalent group of a substituted or unsubstituted condensed polycyclicaromatic, Ar4 represents a substituted or unsubstituted aromatichydrocarbon group, a substituted or unsubstituted aromatic heterocyclicgroup, or a substituted or unsubstituted condensed polycyclic aromaticgroup,

wherein R9 and R10 may be the same or different, and represent afluorine atom, a chlorine atom, cyano, trifluoromethyl, nitro, linear orbranched alkyl of 1 to 6 carbon atoms, cycloalkyl of 5 to 10 carbonatoms, linear or branched alkyloxy of 1 to 6 carbon atoms, cycloalkyloxyof 5 to 10 carbon atoms, a substituted or unsubstituted aromatichydrocarbon group, a substituted or unsubstituted aromatic heterocyclicgroup, a substituted or unsubstituted condensed polycyclic aromaticgroup, or substituted or unsubstituted aryloxy, r9 and r10 represent 0or an integer of 1 to 3, C represents a divalent group of a substitutedor unsubstituted aromatic hydrocarbon, a divalent group of a substitutedor unsubstituted aromatic heterocyclic ring, or a divalent group of asubstituted or unsubstituted condensed polycyclic aromatic, Ar5represents a substituted or unsubstituted aromatic hydrocarbon group, asubstituted or unsubstituted aromatic heterocyclic group, or asubstituted or unsubstituted condensed polycyclic aromatic group, W, X,Y, and Z represent a carbon atom or a nitrogen atom, where only one ofW, X, Y, and Z is a nitrogen atom, and, in this case, the nitrogen atomdoes not have the substituent R9.
 3. The organic electroluminescentdevice of claim 1 comprising a pair of electrodes, and a plurality oforganic layers sandwiched between the pair of electrodes and including aphosphorescent light-emitting material-containing light emitting layerand an electron blocking layer, wherein a compound of the followinggeneral formula (1″) having a carbazole ring structure is used as aconstituent material of the electron blocking layer,

wherein R1, R2, R3, R4, R5, and R6 may be the same or different, andrepresent a fluorine atom, a chlorine atom, cyano, trifluoromethyl,nitro, linear or branched alkyl of 1 to 6 carbon atoms, cycloalkyl of 5to 10 carbon atoms, linear or branched alkyloxy of 1 to 6 carbon atoms,cycloalkyloxy of 5 to 10 carbon atoms, a substituted or unsubstitutedaromatic hydrocarbon group, a substituted or unsubstituted aromaticheterocyclic group, a substituted or unsubstituted condensed polycyclicaromatic group, or substituted or unsubstituted aryloxy, r4 and r5represent 0 or an integer of 1 to 4, r1, r2, r3, and r6 represent 0 oran integer of 1 to 3, Ar1, Ar2, and Ar3 may be the same or different,and represent a substituted or unsubstituted aromatic hydrocarbon group,a substituted or unsubstituted aromatic heterocyclic group, or asubstituted or unsubstituted condensed polycyclic aromatic group.
 4. Theorganic electroluminescent device according to claim 1, wherein thephosphorescent light-emitting material is a metal complex that containsiridium or platinum.
 5. The organic electroluminescent device accordingto claim 2, wherein the phosphorescent light-emitting material is ametal complex that contains iridium or platinum.
 6. The organicelectroluminescent device according to claim 3, wherein thephosphorescent light-emitting material is a metal complex that containsiridium or platinum.